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Lymphocytic interstitial pneumonitis (LIP)

LIP is a non-infectious pulmonary disorder caused by white cell infiltration into alveolae. It is most common in children over 2 years old, and is a clinical stage criterion which is an indication for starting ART.

LIP is common in children (it occurs in at least 40% of children with perinatal HIV), but rare in adults (it occurs in about 3% of adults with HIV). Various studies in Africa have documented a 30–40% prevalence of LIP in HIV-infected children, and up to 60% prevalence in those with chronic lung disease. LIP is often mistaken for pulmonary TB (miliary) because of the chronic cough and the miliary-like pattern on chest X-ray.

Pathogenesis: Possible explanations for LIP include a co-infection of the lungs by HIV and Epstein–Barr virus (EBV), leading to immune stimulation with lymphoid infiltration and chronic inflammation.

The child is often asymptomatic in the early stages, but may later have a mild persistent cough, with or without difficulty in breathing, bilateral parotid swelling, persistent generalised lymphadenopathy, poor growth, hepatomegaly and other signs of heart failure (tender hepatomegaly, bilateral pitting pedal oedema, loud second heart sound and finger clubbing). Chest auscultation may be normal, or there may be widespread crackles. It may produce severe ventilatory perfusion mismatch with hypoxaemia, but may be asymptomatic.

There is an increased risk of lower respiratory tract infection, including bronchiectasis. It is also associated with parotid, adenoid and tonsillar enlargement (and may produce sleep-related upper airway obstruction; see Section 5.1.D).

LIP may be mistaken for miliary TB, but the child is systematically too well.

Suspect LIP if the chest X-ray shows a bilateral reticulo- nodular interstitial pattern that is prominent in the lower lobes, nodules less than 5 mm in diameter, a single patchy alveolar opacity, hyperinflation or isolated bullae. It must be distinguished from pulmonary tuberculosis and bilateral hilar adenopathy (See Figure 6.2.D.4).  Chest x-ray diffuse infiltrations and hilar lymphadeopathy persisting for more than 2 months despite antibiotic treatment are also a clue.

x-ray appearances are often more severe than the clinical features.


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FIGURE 6.2.D.5 Pneumocystis jiroveci pneumonia (PCP): typical is a ground glass appearance.


  

 

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